Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms

被引：24

作者：

Cremonesi, L

Cozzi, A

Girelli, D

Ferrari, F

Fermo, I

Foglieni, B

Levi, S

Bozzini, C

Camparini, M

Ferrari, M

Arosio, P

机构：

[1] IRCCS H San Raffaele, Gen Diag Human Pathol Unit, I-20132 Milan, Italy

[2] IRCCS H San Raffaele, Prot Engn Unit, I-20132 Milan, Italy

[3] Univ Verona, Dept Clin & Expt Med, I-37134 Verona, Italy

[4] IRCCS H San Raffaele, Separat Tech Unit, I-20132 Milan, Italy

[5] Univ Parma, Sect Ophthalmol, I-43100 Parma, Italy

[6] Univ Brescia, Fac Med, Sect Chem, I-25100 Brescia, Italy

来源：

JOURNAL OF MEDICAL GENETICS | 2004年 / 41卷 / 06期

关键词：

D O I：

10.1136/jmg.2003.011718

中图分类号：

Q3 [遗传学];

学科分类号：

071007 [遗传学]; 090102 [作物遗传育种];

摘要：

[No abstract available]

引用

页数：3

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